Tag | Content |
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EnhancerAtlas ID | HS182-01324 | Organism | Homo sapiens | Tissue/cell | Spleen | Coordinate | chr1:150025700-150026770 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr1:150026517-150026528 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr1:150026517-150026528 | GGTGACTCATG | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr1:150026573-150026588 | GAGGTCAGGAGTTCA | + | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 150025873 | 150026018 | chr1 | 150026380 | 150026614 |
| Enhancer Sequence | GCATATATGC AGCCAACGGA CATATGAAAA AAAGCTCAAT ATCACCGATC ATTAGAGAAA 60 TGCAAATCAA AACCACAATG AGATACCATC TCACACCAGT CAGAATGGCC ATTATTAAAA 120 AGTCAGCTCT TTCCCATCTT ACAAGATGGA GGGTGAACAA GTTGAGAAGC CAGATACTAA 180 AGAGAAGAAA CCTGAAGTCA AGAAGGCTGA TGCTGGTGGC AAGGTGAAAA AGGGTAACCT 240 CAAGGCTAAG AAGCCCAAGA ACAGGAAGCC CCATTGCAGT CAAAATCCTG TCATTGTCAG 300 AGGGATTGGC AGATATTCTC CATCTGCTAT GTATTCCAGA AAGGCCACGT GCAAGAGGAA 360 GTACTCAGCT GTGAAATCCA AGGTTGAAAA GCAAAAGGAG AAGTTTCCTG CAACTATTAC 420 AAAACCAGCT GGTGGTGGCA AGAACGGTGG TACGCAGGTG GTTAAACTTT GCAAAATGCC 480 TACATATTAT CTTACTGAAG ATGTGCTTTC AAAGCTGTTG AGCCAAGGAA AAAAACCCTT 540 CAGTCAGCAC ATGAGAAAAC TGTGAGCCAG GATCACTCCC AAGACCATTC TGATCATCCT 600 CACTGAAAGC CACAGGGGCA AGAGGGTGAT TTTCCTGAAG CAGCTGGCTA GTGGCTGGTT 660 ACTTGTGACT GGACCTCTGG TCCTCAATCA AGTTCCTCTA CAAAGAACAC ACCAGAAATC 720 TGTCATTGCC ACCTCAGCCA AAATTGATAT CAGCAATGTA AAAATCCCAA AACATCTTAC 780 TGATACTTAC TTCAAGAAGA AGCTGCAGGC AGGGCATGGT GACTCATGTC TGTAATCCCA 840 GCACTTTGGG AGGCCAAAGC AGGCAAATCA CTTGAGGTCA GGAGTTCAAG ACCAGCACGG 900 CCAACATGGT GAAATCCTGT CTCTACTAAA AATACAAAAA TTAGCCGGGT GTGGTGGCAT 960 GGGCCTGTAA TCCCAGCTAC TTGGGAGGCT GAGGCAGGAG AATCTCTTGA ACTCAGGAGG 1020 CAGAGGTTGC AGTGAGCCCA GAGCGTGCCA CTGCGCTTCA GCCTGGGTGA 1070
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